Recall Z-1530-2016— Acorn Stairlifts Inc
Class II · Terminated
Class II FDA medical device recall by Acorn Stairlifts Inc, initiated 2016-02-17, terminated 2019-01-29. FDA's recall record names no specific 510(k) clearance for this event. Product: Acorn 180 Curved Stairlift. Reason: Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break..
- Recalling firm
- Acorn Stairlifts Inc
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-02-17
- Terminated
- 2019-01-29
- Firm location
- Orlando, FL, United States
Product description
Acorn 180 Curved Stairlift
Reason for recall
Aluminum rivets holding the base squab to the framer under prolonged customer use were seen to elongate and subsequently break.
Data sourced from openFDA. This site is unofficial and independent of the FDA.